ClinVar Miner

Submissions for variant NM_020779.4(WDR35):c.*1575_*1576dup

gnomAD frequency: 0.01057  dbSNP: rs202074829
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000337571 SCV000425921 likely benign Cranioectodermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000408274 SCV000425922 likely benign Short rib-polydactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing

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